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Gene CSF3R
Variant S669G
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CSF3R S669G lies within the cytoplasmic domain of the Csf3r protein (UniProt.org). S669G has not been characterized in the scientific literature and therefore, its effect on Csf3r protein function is unknown (PubMed, Aug 2024).
Associated Drug Resistance
Category Variants Paths

CSF3R mutant CSF3R S669G

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Transcript NM_000760.4
gDNA chr1:g.36467265T>C
cDNA c.2005A>G
Protein p.S669G
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017000370 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
XM_017000370.1 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
XM_047446753.1 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
XM_011540748 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_156039.3 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_000760.4 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_156039 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_156039.3 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_000760 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_000760.3 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
XM_011540748.3 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_172313.2 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_172313 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38
NM_172313.3 chr1:g.36467265T>C c.2005A>G p.S669G RefSeq GRCh38/hg38

Filtering

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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  • Click on any column header arrows to sort by that column
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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries